Success Metrics

Clinical Success Rate
76.9%

Based on 10 completed trials

Completion Rate
77%(10/13)
Active Trials
0(0%)
Results Posted
100%(10 trials)
Terminated
3(21%)

Phase Distribution

Ph phase_2
6
43%
Ph phase_1
2
14%
Ph phase_3
6
43%

Phase Distribution

2

Early Stage

6

Mid Stage

6

Late Stage

Phase Distribution14 total trials
Phase 1Safety & dosage
2(14.3%)
Phase 2Efficacy & side effects
6(42.9%)
Phase 3Large-scale testing
6(42.9%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

71.4%

10 of 14 finished

Non-Completion Rate

28.6%

4 ended early

Currently Active

0

trials recruiting

Total Trials

14

all time

Status Distribution
Completed(10)
Terminated(4)

Detailed Status

Completed10
Terminated3
Withdrawn1

Development Timeline

Analytics

Development Status

Total Trials
14
Active
0
Success Rate
76.9%
Most Advanced
Phase 3

Trials by Phase

Phase 12 (14.3%)
Phase 26 (42.9%)
Phase 36 (42.9%)

Trials by Status

terminated321%
completed1071%
withdrawn17%

Recent Activity

Clinical Trials (14)

Showing 14 of 14 trials
NCT05187403Phase 1

A Study of Laquinimod Eye-drops in Healthy Participants

Completed
NCT01085084Phase 2

A Study of Laquinimod in Participants With Systemic Lupus Erythematosus (SLE) Active Lupus Arthritis

Completed
NCT00605215Phase 3

BRAVO Study: Laquinimod Double-blind Placebo-controlled Study in Participants With Relapsing-Remitting Multiple Sclerosis (RRMS) With a Rater Blinded Reference Arm of Interferon β-1a (Avonex®)

Completed
NCT02284568Phase 2

A Phase 2 Clinical Study in Subjects With Primary Progressive Multiple Sclerosis to Assess the Efficacy, Safety and Tolerability of Two Oral Doses of Laquinimod Either of 0.6 mg/Day or 1.5mg/Day (Experimental Drug) as Compared to Placebo

Completed
NCT01085097Phase 2

A Study of Laquinimod in Participants With Systemic Lupus Erythematosus (SLE) Active Lupus Nephritis

Completed
NCT01047319Phase 3

A Study to Evaluate the Long-term Safety, Tolerability and Effect of Daily Oral Laquinimod 0.6 mg on Disease Course in Subjects With Relapsing Multiple Sclerosis

Terminated
NCT00988052Phase 3

A Study To Evaluate the Long-Term Safety, Tolerability and Effect on Disease Course

Terminated
NCT01707992Phase 3

The Efficacy, Safety, and Tolerability of Laquinimod in Participants With Relapsing Remitting Multiple Sclerosis (RRMS)

Completed
NCT02085863Phase 1

A Phase I Study in Young Healthy Women to Investigate the Effects of Laquinimod on Standard Oral Contraceptive When Both Treatments Are Given Together

Completed
NCT01975298Phase 3

A Study to Evaluate 2 Doses Of Oral Administration Of Laquinimod Compared to Interferon ß-1a Administered by Injection in Participants With Relapsing Remitting Multiple Sclerosis (RRMS)

Withdrawn
NCT00509145Phase 3

Safety and Efficacy of Orally Administered Laquinimod Versus Placebo for Treatment of Relapsing Remitting Multiple Sclerosis (RRMS)

Completed
NCT02215616Phase 2

A Clinical Study in Participants With Huntington's Disease (HD) to Assess Efficacy and Safety of Three Oral Doses of Laquinimod

Completed
NCT00745615Phase 2

An Extension Study of LAQ/5062 Exploring the Long Term Safety, Tolerability and Clinical Effect Parameters During the Disease

Terminated
NCT00737932Phase 2

Laquinimod Phase IIa Study in Active Crohn's Disease

Completed

All 14 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
14